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Intramuscular SARS-CoV-2 vaccines elicit varying degrees of plasma and salivary antibody responses as compared to natural infection
George Ronald Nahass; Rachel E Salomon-Shulman; Grace Blacker; Kazim Haider; Rich Brotherton; Kristine Teague; Ying Ying Yiu; Rachel E. Brewer; Sarah Danielle Galloway; Paige Hansen; Gabriel Marquez-Arreguin; Salma Sheikh-Mohamed; Gary Y.C. Chao; Baweleta Isho; Evan Do; Iris Chang; Theo Snow; Alexandra S. Lee; - STANFORD COVID-19 BIOBANK; Monali Manohar; Samuel Yang; Andra L. Blomkalns; Angela J. Rogers; Allison McGeer; Anne-Claude Gingras; Sharon Straus; Phillip Grant; Kari C. Nadeau; Catherine A. Blish; Jennifer L. Gommerman; Erin C. Sanders; Irving L. Weissman; Michal Caspi Tal.
Afiliação
  • George Ronald Nahass; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Rachel E Salomon-Shulman; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Grace Blacker; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Kazim Haider; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Rich Brotherton; Clinical and Translational Research Unit (CTRU), Stanford University School of Medicine, Stanford, CA, USA
  • Kristine Teague; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Ying Ying Yiu; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Rachel E. Brewer; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Sarah Danielle Galloway; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Paige Hansen; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA; Department of
  • Gabriel Marquez-Arreguin; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine
  • Salma Sheikh-Mohamed; Department of Immunology, University of Toronto, Toronto, Canada
  • Gary Y.C. Chao; Department of Immunology, University of Toronto, Toronto, Canada
  • Baweleta Isho; Department of Immunology, University of Toronto, Toronto, Canada
  • Evan Do; Sean N. Parker Center for Allergy and Asthma Research, Stanford University School Medicine, Stanford, CA, USA
  • Iris Chang; Sean N. Parker Center for Allergy and Asthma Research, Stanford University School Medicine, Stanford, CA, USA
  • Theo Snow; Sean N. Parker Center for Allergy and Asthma Research, Stanford University School Medicine, Stanford, CA, USA
  • Alexandra S. Lee; Sean N. Parker Center for Allergy and Asthma Research, Stanford University School Medicine, Stanford, CA, USA
  • - STANFORD COVID-19 BIOBANK; Stanford COVID-19 Biobank, Stanford University School of Medicine, Stanford, CA, USA
  • Monali Manohar; Sean N. Parker Center for Allergy and Asthma Research, Stanford University School Medicine, Stanford, CA, USA
  • Samuel Yang; Department of Emergency Medicine, Stanford University School of Medicine, Stanford, CA, USA
  • Andra L. Blomkalns; Department of Emergency Medicine, Stanford University School of Medicine, Stanford, CA, USA
  • Angela J. Rogers; Department of Medicine, Stanford University School of Medicine, Stanford, CA USA
  • Allison McGeer; Lunenfeld-Tanenbaum Research Institute and Mount Sinai Hospital, Toronto, Canada Department of Immunology, University of Toronto, Toronto, Canada
  • Anne-Claude Gingras; Lunenfeld-Tanenbaum Research Institute and Mount Sinai Hospital, Toronto, Canada Department of Immunology, University of Toronto, Toronto, Canada; Department of
  • Sharon Straus; Li Ka Shing Knowledge Institute of St. Michael?s Hospital, Unity Health Toronto, Canada
  • Phillip Grant; Department of Medicine, Stanford University School of Medicine, Stanford, CA USA
  • Kari C. Nadeau; Sean N. Parker Center for Allergy and Asthma Research, Stanford University School Medicine, Stanford, CA, USA
  • Catherine A. Blish; Department of Medicine, Stanford University School of Medicine, Stanford, CA USA
  • Jennifer L. Gommerman; Department of Immunology, University of Toronto, Toronto, Canada
  • Erin C. Sanders; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA; Department of
  • Irving L. Weissman; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
  • Michal Caspi Tal; Institute for Stem Cell Biology and Regenerative Medicine and the Ludwig Cancer Center, Stanford University School of Medicine, Stanford, CA, USA
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21262168
ABSTRACT
Vaccination induced antibody and T-cell immune responses are important for systemic protection from COVID-19. Because SARS-CoV-2 infects and is transmitted by oral-pharyngeal mucosa, we wished to test mucosal antibodies elicited by natural infection or intramuscular vaccine injection. In a non-randomized observational study, we measured antibodies against the SARS-CoV-2 RBD in plasma and saliva from convalescent or vaccinated individuals and tested their neutralizing potential using a replication competent rVSV-eGFP-SARS-CoV-2. We found IgG and IgA anti-RBD antibodies as well as neutralizing activity in convalescent plasma and saliva. Two doses of mRNA vaccination (BNT162b2 or mRNA-1273) induced high levels of IgG anti-RBD in saliva, a subset of whom also had IgA, and significant neutralizing activity. We detected anti-RBD IgG and IgA with significant neutralizing potential in the plasma of single dose Ad26.COV2.S vaccinated individuals, and we detected slight amounts of anti-RBD antibodies in matched saliva. The role of salivary antibodies in protection against SARS-CoV-2 infection is unknown and merits further investigation. This study was not designed to, nor did it study the full kinetics of the antibody response or protection from infection, nor did it address variants of SARS-CoV-2.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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